EP3830545A1 - Systems and methods for detecting particles in a fluid channel - Google Patents
Systems and methods for detecting particles in a fluid channelInfo
- Publication number
- EP3830545A1 EP3830545A1 EP19752863.1A EP19752863A EP3830545A1 EP 3830545 A1 EP3830545 A1 EP 3830545A1 EP 19752863 A EP19752863 A EP 19752863A EP 3830545 A1 EP3830545 A1 EP 3830545A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- channel
- particle
- sensor
- droplet
- substrate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000002245 particle Substances 0.000 title claims abstract description 175
- 238000000034 method Methods 0.000 title claims abstract description 39
- 239000012530 fluid Substances 0.000 title abstract description 5
- 230000005670 electromagnetic radiation Effects 0.000 claims abstract description 28
- 239000000758 substrate Substances 0.000 claims description 73
- 230000003287 optical effect Effects 0.000 claims description 26
- 230000003595 spectral effect Effects 0.000 claims description 6
- 238000012512 characterization method Methods 0.000 claims description 4
- 230000000295 complement effect Effects 0.000 claims description 4
- 239000004065 semiconductor Substances 0.000 claims description 4
- 238000001228 spectrum Methods 0.000 claims description 4
- 238000000862 absorption spectrum Methods 0.000 claims description 3
- 238000000149 argon plasma sintering Methods 0.000 claims description 3
- 230000008859 change Effects 0.000 claims description 3
- 239000002609 medium Substances 0.000 description 45
- 239000000463 material Substances 0.000 description 21
- 238000005286 illumination Methods 0.000 description 9
- 239000003921 oil Substances 0.000 description 6
- 230000005855 radiation Effects 0.000 description 6
- 230000009471 action Effects 0.000 description 5
- 210000004027 cell Anatomy 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 238000000206 photolithography Methods 0.000 description 5
- 238000001039 wet etching Methods 0.000 description 5
- 238000004458 analytical method Methods 0.000 description 4
- 238000001312 dry etching Methods 0.000 description 4
- 230000005684 electric field Effects 0.000 description 4
- 238000001943 fluorescence-activated cell sorting Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000001459 lithography Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 230000001133 acceleration Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000002502 liposome Substances 0.000 description 3
- 238000001020 plasma etching Methods 0.000 description 3
- 230000008901 benefit Effects 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 238000010894 electron beam technology Methods 0.000 description 2
- 230000005284 excitation Effects 0.000 description 2
- 238000002032 lab-on-a-chip Methods 0.000 description 2
- 238000010329 laser etching Methods 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000001000 micrograph Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 238000002174 soft lithography Methods 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 239000012780 transparent material Substances 0.000 description 2
- 238000003631 wet chemical etching Methods 0.000 description 2
- 238000010146 3D printing Methods 0.000 description 1
- JBRZTFJDHDCESZ-UHFFFAOYSA-N AsGa Chemical compound [As]#[Ga] JBRZTFJDHDCESZ-UHFFFAOYSA-N 0.000 description 1
- 229910001218 Gallium arsenide Inorganic materials 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000004720 dielectrophoresis Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 210000001808 exosome Anatomy 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- 238000011005 laboratory method Methods 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000009740 moulding (composite fabrication) Methods 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- 239000013307 optical fiber Substances 0.000 description 1
- -1 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000307 polymer substrate Polymers 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 230000002250 progressing effect Effects 0.000 description 1
- 239000002096 quantum dot Substances 0.000 description 1
- 238000010223 real-time analysis Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 229910002076 stabilized zirconia Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000004416 surface enhanced Raman spectroscopy Methods 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
- G01N15/02—Investigating particle size or size distribution
- G01N15/0205—Investigating particle size or size distribution by optical means
- G01N15/0211—Investigating a scatter or diffraction pattern
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
- G01N15/10—Investigating individual particles
- G01N15/14—Optical investigation techniques, e.g. flow cytometry
- G01N15/1434—Optical arrangements
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
- G01N15/10—Investigating individual particles
- G01N15/14—Optical investigation techniques, e.g. flow cytometry
- G01N15/1456—Optical investigation techniques, e.g. flow cytometry without spatial resolution of the texture or inner structure of the particle, e.g. processing of pulse signals
- G01N15/1459—Optical investigation techniques, e.g. flow cytometry without spatial resolution of the texture or inner structure of the particle, e.g. processing of pulse signals the analysis being performed on a sample stream
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
- G01N15/01—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials specially adapted for biological cells, e.g. blood cells
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
- G01N15/10—Investigating individual particles
- G01N15/14—Optical investigation techniques, e.g. flow cytometry
- G01N15/149—Optical investigation techniques, e.g. flow cytometry specially adapted for sorting particles, e.g. by their size or optical properties
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
- G01N2015/0023—Investigating dispersion of liquids
- G01N2015/003—Investigating dispersion of liquids in liquids, e.g. emulsion
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
- G01N15/10—Investigating individual particles
- G01N2015/1027—Determining speed or velocity of a particle
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
- G01N15/10—Investigating individual particles
- G01N2015/1028—Sorting particles
Definitions
- Embodiments of the present disclosure include a system for detecting at least one particle or at least one droplet in a channel, including a channel having at least one particle or at least one droplet dispersed in a medium, such that the at least one particle or the at least one droplet is moving from a first end of the channel to a second end of the channel, a source of electromagnetic radiation that illuminates at least a portion of the channel, a sensor to detect the at least one particle or the at least one droplet, wherein the sensor is positioned along the linear axis of the illuminated portion of the channel such that the sensor is substantially parallel to the direction of movement of the at least one particle through the channel, and an optical system that focuses and aligns the illuminated portion of the channel to the sensor.
- the senor is a linear charge-coupled sensor, a linear complementary metal-oxide-semiconductor sensor, any suitable optical sensor, or any combination thereof.
- the channel is positioned in or on a substrate.
- the source of illumination comprises an optical system.
- the system further includes a plurality of particles or droplets and/or a plurality of channels and/or a plurality of linear sensors.
- the sensor and a detector detect the movement and or position of the at least one particle or at least one droplet over a predetermined time and/or distance.
- the optical system comprises a lens selected from the group consisting of a cylindrical lens, or a telecentric lens, or a spherical lens, or an aspheric lens, or any suitable lens, or any combination thereof.
- the sensor can detect spectral information about the particle or the droplet.
- the system can include a sensor positioned within the region of illumination, but perpendicular to the linear axis.
- the substrate and the medium have a similar refractive index.
- signals from the sensor are used to modulate a device that is separate from the system (e.g., a component for sorting the plurality of particles in a channel based on the size, position and/or other characteristics).
- the device that is separate from the system is a component for sorting a plurality of particles in a channel based on size, position, and/or other characteristics.
- the detecting is performed in real time.
- the detecting can include characterizing the at least one particle or the at least one droplet (e.g., identifying the at least one particle or the at least one droplet, recording a velocity of the at least one particle or the at least one droplet, recording a size of the at least one particle or the at least one droplet, recording an absorption spectrum of the at least one particle or the at least one droplet, recording a fluorescent spectrum of the at least one particle or the at least one droplet; recording light scattering of the at least one particle or the at least one droplet, recording a refractive index of the at least one particle or the at least one droplet, any suitable characterization technique, or any combination thereof).
- characterizing the at least one particle or the at least one droplet e.g., identifying the at least one particle or the at least one droplet, recording a velocity of the at least one particle or the at least one droplet, recording a size of the at least one particle or the at least one droplet, recording an absorption spectrum of the at least one particle or the at least one drop
- the method further includes sorting a plurality of particles or droplets in real time according to particle or droplet identification, particle or droplet size, or any suitable attribute.
- the sorting can be performed by actuating at least an electrode, valve or other component that may be used to change a direction of particle flow through the channel.
- Figure 2 is an illustration of a micrograph showing droplets flowing in a channel according to an embodiment described herein.
- Figure 3 is a schematic depicting a droplet flowing past a sensor according to an embodiment described herein.
- Figure 5 is an illustration of a digital image showing droplets flowing in a channel according to an embodiment described herein.
- Figure 8 is a graph showing data detected by a sensor adjacent to a channel according to an embodiment described herein.
- Figure 9A is an illustration of a digital image showing droplets flowing in a channel and an accompanying graph showing data detected by a sensor adjacent to the channel according to an embodiment described herein.
- Figure 9B is an illustration of a digital image showing droplets flowing in a channel and an accompanying graph showing data detected by a sensor adjacent to the channel according to an embodiment described herein.
- Certain aspects and features of the present disclosure relate to tracking particles or droplets in a channel and in some embodiments, specifically to fluorescence activated cell sorting (FACS).
- FACS fluorescence activated cell sorting
- the channel can be a microfluidic channel disposed onto or within a substrate.
- the channel can further include a medium in which the particles or droplets can be carried (i.e., such that the particles or droplets flow through the channel in the medium).
- the channel and the medium can have a similar refractive index such that they appear translucent or transparent to each other, and when illuminated by electromagnetic radiation are simultaneously translucent or transparent to the radiation.
- At least two of the substrate, the channel, and/or the medium are translucent or transparent. In some cases, at least two of the substrate, the channel, and/or the medium can have a similar refractive index such that they are, or appear translucent or transparent to each other.
- the particles or droplets can have a refractive index substantially different from that of the substrate, the channel, and/or the medium, such that the particles or droplets interfere with the electromagnetic radiation.
- a sensor can be disposed adjacent to the channel to record the electromagnetic radiation. The sensor can be attached to a system for identifying, tracking, and sorting the particles or droplets.
- a plurality of channels can be combined to form a network. It is noted that description embodiments described for compositions may also be incorporated in methods and/or systems and vice versa.
- the term "and/or" when used in a list of two or more items, means that any one of the listed items can be employed by itself or in combination with any one or more of the listed items.
- the expression “A and/or B” is intended to mean either or both of A and B, i.e. A alone, B alone or A and B in combination.
- the expression “A, B and/or C” is intended to mean A alone, B alone, C alone, A and B in combination, A and C in combination, B and C in combination or A, B, and C in combination.
- range format Various aspects of this disclosure are presented in a range format. It should be understood that the description in range format is merely for convenience and brevity and should not be construed as an inflexible limitation on the scope of the disclosure. Accordingly, the description of a range should be considered to have specifically disclosed all the possible sub-ranges as well as individual numerical values within that range. For example, description of a range such as from 1 to 6 should be considered to have specifically disclosed sub-ranges such as from 1 to 3, from 1 to 4, from 1 to 5, from 2 to 4, from 2 to 6, from 3 to 6 etc., as well as individual numbers within that range, for example, 1, 2, 3, 4, 5, and 6. This applies regardless of the breadth of the range.
- a translucent material is a material wherein a fraction of impinging light diffracted above 2.5° of an incident angle (referred to as“haze”) exceeds 30%.
- haze a fraction of impinging light diffracted above 2.5° of an incident angle
- a transparent material is a material wherein greater than 75% of ultraviolet light, visible light and near-infrared radiation (e.g., electromagnetic radiation having a wavelength from about 200 nm to about 2500 nm) can transmit through the transparent material.
- visible light and near-infrared radiation e.g., electromagnetic radiation having a wavelength from about 200 nm to about 2500 nm
- two materials and/or media having equal or similar refractive indices refract light similarly with respect to each other, thus allowing the light to pass through the two materials/media uninhibited, providing a substantially transparent pair.
- glass and air have similar refractive indices, thus light passes through glass and air uninhibited.
- two media/materials have significantly different refractive indices, light transmitting from a first media/material to a second media/material is refracted in directions significantly differently as to inhibit light transmission through the system.
- a droplet is a self-contained volume of a first medium dispersed, suspended, or otherwise included in a second medium.
- the first medium of the droplet is a liquid and the second medium is either a liquid or a gas, though it need not be.
- the droplet may be homogeneous or heterogeneous (i.e., include other materials within the droplet such as solid particles, gas bubbles, miscible liquids, immiscible liquids, or the like).
- the droplet may be an oil droplet in an aqueous medium, a water droplet in an oil medium, a soap bubble in air, or the like).
- a system for detecting at least one particle or at least one droplet in a channel including a channel having at least one particle or at least one droplet dispersed in a medium, such that the at least one particle or the at least one droplet (i.e., the particle or the droplet) is moving from a first end of the channel to a second end of the channel, a source of electromagnetic radiation that illuminates at least a portion of the channel, a sensor to detect the particle or the droplet, wherein the sensor is positioned along the linear axis of the illuminated portion of the channel such that the sensor is substantially parallel to the direction of movement of the particle through the channel, and an optical system that focuses and aligns the illuminated portion of the channel to the sensor.
- the channel can be created by creating at least a first half of a channel in a first substrate and creating a second half of a channel in a second substrate, and aligning and joining the first substrate to the second substrate such that the first half of the channel and the second half of the channel form a complete channel encased within the first substrate and the second substrate.
- the channel can be at least partially exposed to the environment outside of the substrate.
- a portion of the substrate can be removed in a predetermined pattern creating an exposed channel positioned at least partially within the substrate, such that any medium and/or particles or droplets (e.g., cells, liposomes, or the like) are exposed to the environment outside of the substrate when flowing through the channel.
- the portion of the substrate can be removed by any one of reactive ion etching (i.e., dry etching), wet chemical etching (i.e., wet etching), electron beam (E-beam) lithography, photolithography (e.g., photolithography employing dry etching and/or wet etching), laser etching, any suitable material removal technique, or any combination thereof.
- the channel can be fabricated on the substrate.
- the channel can be created by depositing a material onto the substrate, removing at least a portion of the material in a predetermined pattern (e.g., a channel or a network of channels) to create a channel within the material deposited onto the substrate.
- the portion of the material deposited onto the substrate can be removed by any one of reactive ion etching (i.e., dry etching), wet chemical etching (i.e., wet etching), electron beam (E-beam) lithography, photolithography (e.g., photolithography employing dry etching and/or wet etching), laser etching, soft lithography, two- photon lithography, forming the channel around a sacrificial template, any suitable material removal technique, or any combination thereof.
- the channel can be created by three dimensional (3D) printing.
- round channels can have a diameter of 1 nm, 5 nm, 10 nm, 20 nm, 30 nm, 40 nm, 50 nm, 60 nm, 70 nm, 80 nm, 90 nm, 100 nm, 200 nm, 300 nm, 400 nm, 500 nm, 600 nm, 700 nm, 800 nm, 900 nm, 1 pm, 5 pm, 10 pm, 20 pm, 30 pm, 40 pm, 50 pm, 60 pm, 70 pm, 80 pm, 90 pm, 100 pm, 200 pm, 300 pm, 400 pm, 500 pm, 600 pm, 700 pm, 800 pm, 900 pm, 1 mm, 5 mm, 10 mm, 20 mm, 30 mm, 40 mm, 50 mm, 60 mm, 70 mm, 80 mm, 90 mm, 1 cm, or anywhere in between.
- a line scan can be taken along the linear axis 210 of the channel 110.
- contrast changes can be recorded to determine the location of the droplet 120, a particle, a liposome, or any suitable material dispersed in a medium flowing within the channel 110.
- data recorded from the sensor can be presented as a kymograph (see Figure 4).
- the y-axis represents time and the x-axis represents position of the droplet 120.
- the kymograph represents the progression of the droplet 120 as recorded by the sensor in the example of Figure 3.
- the progression of the droplet 120 is depicted as a single line, thus the kymograph in the example of Figure 4 depicts the progression of 35 droplets.
- Velocity of the droplet 120 is represented by the slope of the line (e.g., a steeper slope indicates a slower droplet).
- velocity of the droplet 120 was varied as it progressed through the channel 110.
- Illustration 3 is the system of any preceding or subsequent illustration, wherein the channel is positioned in or on a substrate.
- Illustration 4 is the system of any preceding or subsequent illustration, wherein a source of electromagnetic radiation comprises an optical system.
- Illustration 9 is the system of any preceding or subsequent illustration, wherein the particle is a droplet.
- Illustration 11 is the system of any preceding or subsequent illustration, wherein the at least two of the substrate, the channel and the medium have a similar refractive index.
- Illustration 16 is the method of any preceding or subsequent illustration, further comprising characterizing the at least one particle.
- Illustration 18 is the method of any preceding or subsequent illustration, further comprising sorting a plurality of particles in real time.
- Illustration 19 is the method of any preceding or subsequent illustration, wherein the sorting is performed according to particle identification, particle size, any suitable attribute, or any combination thereof.
Landscapes
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
Abstract
Description
Claims
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201862714198P | 2018-08-03 | 2018-08-03 | |
US201862720248P | 2018-08-21 | 2018-08-21 | |
PCT/US2019/044622 WO2020028638A1 (en) | 2018-08-03 | 2019-08-01 | Systems and methods for detecting particles in a fluid channel |
Publications (2)
Publication Number | Publication Date |
---|---|
EP3830545A1 true EP3830545A1 (en) | 2021-06-09 |
EP3830545B1 EP3830545B1 (en) | 2024-10-02 |
Family
ID=67614707
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19752863.1A Active EP3830545B1 (en) | 2018-08-03 | 2019-08-01 | Systems and methods for detecting particles in a fluid channel |
Country Status (3)
Country | Link |
---|---|
US (1) | US11480508B2 (en) |
EP (1) | EP3830545B1 (en) |
WO (1) | WO2020028638A1 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20220339674A1 (en) * | 2021-04-22 | 2022-10-27 | MicroRecycling Systems LLC | Apparatus and method for classifying parts for separating or sorting a set of parts |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007051170A2 (en) | 2005-10-28 | 2007-05-03 | The Regents Of The University Of California | Apparatus and method for improved optical detection of particles in fluid |
WO2008144496A1 (en) * | 2007-05-18 | 2008-11-27 | Vanderbilt University | Improved interferometric detection system and method |
US8528589B2 (en) * | 2009-03-23 | 2013-09-10 | Raindance Technologies, Inc. | Manipulation of microfluidic droplets |
US9068916B2 (en) | 2010-03-15 | 2015-06-30 | Bio-Rad Laboratories, Inc. | Microassembled imaging flow cytometer |
FR2991457B1 (en) * | 2012-06-01 | 2014-07-18 | Commissariat Energie Atomique | METHOD AND SYSTEM FOR CHARACTERIZING THE SPEED OF DISPLACEMENT OF PARTICLES CONTAINED IN A LIQUID, SUCH AS BLOOD PARTICULATES |
CN107532991A (en) * | 2015-03-10 | 2018-01-02 | 迈克必斯生物系统公司 | For sorting the mthods, systems and devices with Treatment Analysis thing |
-
2019
- 2019-08-01 US US16/529,006 patent/US11480508B2/en active Active
- 2019-08-01 WO PCT/US2019/044622 patent/WO2020028638A1/en unknown
- 2019-08-01 EP EP19752863.1A patent/EP3830545B1/en active Active
Also Published As
Publication number | Publication date |
---|---|
US11480508B2 (en) | 2022-10-25 |
EP3830545B1 (en) | 2024-10-02 |
WO2020028638A1 (en) | 2020-02-06 |
US20200041399A1 (en) | 2020-02-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP3164692B1 (en) | Flow cytometry system and method | |
JP6031178B2 (en) | Disposable chip type flow cell and cell sorter using the same | |
Rosenauer et al. | Miniaturized flow cytometer with 3D hydrodynamic particle focusing and integrated optical elements applying silicon photodiodes | |
US9594071B2 (en) | Device and method for laser analysis and separation (LAS) of particles | |
US20170299492A1 (en) | Method, device and system for hydrodynamic flow focusing | |
US20070207061A1 (en) | Optofluidic microscope device | |
Barat et al. | Simultaneous high speed optical and impedance analysis of single particles with a microfluidic cytometer | |
US20050271548A1 (en) | Optofluidic microscope device | |
US20060171846A1 (en) | Microfluidic systems incorporating integrated optical waveguides | |
WO2016100954A1 (en) | Flow cytometry using hydrodynamically planar flow | |
US20060073076A1 (en) | Cell analyzing and segregating device | |
US11561164B2 (en) | Microfluidic chip device for optical force measurements and cell imaging using microfluidic chip configuration and dynamics | |
JP2024020465A (en) | Microfluidic chip device for optical force measurement and cell imaging using microfluidic chip configuration and dynamics | |
US11480508B2 (en) | Systems and methods for detecting particles in a fluid channel | |
US20050067337A1 (en) | Laser optical separator and method for separating colloidal suspensions | |
EP3950133A1 (en) | Microfluidic chip and device for determining the physical properties and/or the chemical nature of solid microplastic particles suspended in a liquid sample | |
WO2016099538A1 (en) | Flow cytometry using hydrodynamically planar flow | |
Goel et al. | Integrated waveguide mixer/splitter for lab-on-a-chip applications |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: UNKNOWN |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE |
|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE |
|
17P | Request for examination filed |
Effective date: 20210201 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
DAV | Request for validation of the european patent (deleted) | ||
DAX | Request for extension of the european patent (deleted) | ||
RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: GUTIERREZ, MICHAEL Inventor name: HOMYK, ANDREW Inventor name: SINHA, SUPRIYO Inventor name: VYAWAHARE, SAURABH |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: EXAMINATION IS IN PROGRESS |
|
17Q | First examination report despatched |
Effective date: 20230622 |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: GRANT OF PATENT IS INTENDED |
|
RIC1 | Information provided on ipc code assigned before grant |
Ipc: G01N 21/64 20060101ALI20240419BHEP Ipc: G01N 21/05 20060101ALI20240419BHEP Ipc: G01N 15/1434 20240101ALI20240419BHEP Ipc: G01N 15/14 20060101ALI20240419BHEP Ipc: G01N 15/00 20060101AFI20240419BHEP |
|
INTG | Intention to grant announced |
Effective date: 20240515 |
|
GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE PATENT HAS BEEN GRANTED |
|
P01 | Opt-out of the competence of the unified patent court (upc) registered |
Free format text: CASE NUMBER: APP_45800/2024 Effective date: 20240807 |
|
RAP3 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: VERILY LIFE SCIENCES LLC |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: FG4D |